CrawlJobs Logo

Clinical Application Manager

circlehealthgroup.co.uk Logo

Circle Health Group

Location Icon

Location:
United Kingdom , Central London

Category Icon

Job Type Icon

Contract Type:
Not provided

Salary Icon

Salary:

Not provided

Job Description:

Circle Health Group is proud to be recognised as one of the UK’s top 5 best big companies to work for as well as top 5 to work for in the health and social care sector. We have an opportunity for a Clinical Application Manager to join their team of staff in the Group IT department. This is a Full time role for 37.5 hours a week. The role holder will be required to cover a flexible shift pattern, Monday to Friday.

Job Responsibility:

  • Lead, mentor, and manage a team of application specialists, providing direction, support, and professional development opportunities
  • Foster a collaborative and inclusive team culture, encouraging knowledge sharing, innovation, and continuous improvement
  • Conduct regular performance evaluations, set clear objectives, and provide constructive feedback to support the growth and development of all team members
  • Deputise for the Head of Clinical Systems, as requested
  • Oversee the development and implementation of strategies to enhance and replace clinical applications to improve workflow efficiency, improve patient care outcomes, and drive innovation in clinical operations through the effective use of technology
  • Manage ongoing maintenance activities to ensure the stability, performance, and security of clinical applications. Continuously optimise applications to meet changing business needs and technological advancements
  • Create, maintain, and revise robust and repeatable testing methodologies that will ensure consistent testing for new upgrades, functionality and systems that will result in identifying, tracking and resolution of issues with suppliers and other involved teams

Requirements:

  • Strong (3+ years) experience in supporting and managing clinically facing IT applications within large (~£250M+ annual revenue, 5,000+ end-users, 20+ different locations) organisations
  • Strong (3+ years) experience in managing teams with complex workloads and evidence of large-scale project delivery
  • Strong (3+ years) experience in service delivery of the IT environment and managing of 3rd party supplier relations
  • Strong up to date knowledge of relevant legislation including data protection, information security and information governance
  • Excellent interpersonal skills and a strong customer and team working ethos, able to build and maintain good, effective working relationships across IT End-Users, Clinicians, Managers, IT team and 3rd Parties
  • Strong, demonstrable analytical and problem-solving skills with data analysis and reporting using pre-built tools
  • Ability to explain/translate highly technical documents to non-technical colleagues
  • Excellent written and verbal communication, and interpersonal skills
  • Experience of mentoring and developing team members
  • Experience of private healthcare based clinical or IT role
  • ITIL Certification
  • Experience in the creation and delivery of application training
  • Highly self-motivated and well organised to deliver results and have a pro-active approach to duties and self-development, setting personal objectives that support the business/team goals
  • Keen and able to learn new technologies
  • Proficient in the use of Microsoft Office tools (Word, Excel, and PowerPoint), service desk management systems and analytical tools (specifically experience using SQL scripting)
What we offer:
  • 25 days holiday per year + bank holidays, increasing to 30 days with service
  • Private Pension Scheme
  • Private Healthcare Scheme for treatment at our hospitals, covering pre-existing medical conditions
  • Friends & Family Hospital Discounts
  • Family Friendly policies, including enhanced Maternity, Paternity & Adoption pay
  • Non-contributory life insurance
  • Staff engagement hub with access to discounts and extensive rewards and voluntary benefits
  • Access to resources, tools and services to support your wellbeing
  • Employee recognition programmes
  • Industry leading training and development opportunities

Additional Information:

Job Posted:
December 27, 2025

Expiration:
December 28, 2025

Employment Type:
Fulltime
Work Type:
Remote work
Job Link Share:

Looking for more opportunities? Search for other job offers that match your skills and interests.

Briefcase Icon

Similar Jobs for Clinical Application Manager

Analyst, Clinical Data Management, Clinical Informatics-Ambulatory

As part of the Epic team, you will be expected to be proficient in all critical ...
Location
Location
United States , Work From Home
Salary
Salary:
83430.00 - 222480.00 USD / Year
https://www.cvshealth.com/ Logo
CVS Health
Expiration Date
March 02, 2026
Flip Icon
Requirements
Requirements
  • Minimum of five (5) years of related experience is required
  • Two or more Epic Certifications: EpicCare Ambulatory, Healthy Planet, Beacon, Willow, Prelude, Cadence, Resolute Professional Billing, HIM (Health Information Management), MyChart, Beaker, Welcome Kiosk, Rover, Haiku, EpicCare Link, Caboodle, SlicerDicer, Bridges, Reporting Workbench, Orders
  • Bachelor's degree is required or equivalent experience
  • Strong experience configuring, designing, and supporting an Epic solution
  • Previous application configuration experience
  • Knowledge of Ambulatory workflows and quality and safety initiatives
  • Experience in test planning & execution, test case development, and meeting project quality requirements
  • Experience working on large projects, strong knowledge of clinical applications and understanding of the healthcare IT industry
  • Understanding of configurable applications and monitoring practices
  • Analytical, problem resolution and interpersonal skills
Job Responsibility
Job Responsibility
  • Design and develop and facilitate deployment of the quality and safety initiatives
  • Oversee build and maintenance of Epic environments, related in particular to Medical Affairs safety efforts
  • Facilitate communication and problem solving sessions to identify, scope and plan for safety mitigation plans
  • Maintain comprehensive documentation of materials and methodologies, user guides, and support resources
  • Create and fulfill EHR use cases, identify business and functional requirements and working closely with IT resources to translate requirements and workflows to technical specifications
  • Lead documentation efforts for discovery and implementation
  • Ensure requirements and future state workflows are clearly defined
  • Support development of Quality and Safety Governance and guidance group supporting both Oak Street Health and all CVS business units
  • Work with across the CVS enterprise to identify tasks and associated business units impacted by quality & safety efforts
  • Support execution of vendor upgrades, system changes and environment maintenance procedures
What we offer
What we offer
  • Affordable medical plan options
  • 401(k) plan with matching company contributions
  • Employee stock purchase plan
  • No-cost wellness screenings
  • Tobacco cessation and weight management programs
  • Confidential counseling and financial coaching
  • Paid time off
  • Flexible work schedules
  • Family leave
  • Dependent care resources
  • Fulltime
Read More
Arrow Right

Associate Director, Clinical Data Management

The Associate Director, Clinical Data Management plays a key role within the Cli...
Location
Location
United States , Waltham
Salary
Salary:
160000.00 - 200000.00 USD / Year
kailera.com Logo
Kailera Therapeutics
Expiration Date
Until further notice
Flip Icon
Requirements
Requirements
  • At least 10 years of experience in clinical data management, including direct collaboration with CROs and data management vendors
  • Comprehensive knowledge of FDA and ICH/GCP regulations and their application to data management processes
  • Proficiency in CDISC standards (CDASH/SDTM), medical coding dictionaries, 21 CFR Part 11 compliance, and industry best practices in clinical data management
  • Exceptional interpersonal, communication, and organizational abilities, with a demonstrated capacity to manage multiple programs and workflows in a dynamic, team-oriented setting
  • Proven success in managing vendor relationships and functional service provider (FSP) partnerships
  • Strong track record of building effective relationships and managing expectations with external partners and vendors
  • Practical experience with electronic Trial Master File (eTMF) systems related to CDM documentation
  • Bachelor’s degree or higher in Life Science or related discipline
Job Responsibility
Job Responsibility
  • Provide project-level leadership for clinical data management (CDM) activities, monitor and report on overall study progress
  • Develop and maintain study timelines and ensure timely delivery of data-related milestones in collaboration with cross-functional teams and external vendors
  • Oversee the creation of study-specific CDM documentation, including eCRF specifications, completion guidelines, edit check specifications, and data management plans—proactively identifying and mitigating risks to data quality and ensuring appropriate filing in the Trial Master File (eTMF)
  • Manage CRO CDM counterparts to ensure compliance with scope of work, contractual agreements, timelines, and quality standards
  • Conduct end-to-end testing of electronic case report forms (eCRFs), including authoring and executing User Acceptance Test (UAT) plans and scripts prior to deployment
  • Develop and execute risk mitigation and action plans as needed to maintain data integrity and operational efficiency
  • Actively participate in internal study team discussions and engage with external stakeholders through vendor teleconferences
  • Serve as a primary liaison to internal partners (Clinical Operations, Biometrics, Safety/Pharmacovigilance, Regulatory Affairs) and external entities (CROs, third-party data vendors)
  • Monitor vendor performance and quality
  • escalate issues to management and implement corrective actions as appropriate
What we offer
What we offer
  • Comprehensive health benefits and tax-advantaged savings accounts
  • Flexible time off, 13 paid holidays, and a companywide year-end shutdown
  • Monthly wellness stipend
  • Generous 401(k) match
  • Disability and life insurance
  • Fulltime
Read More
Arrow Right

Ultrasound Clinical Application Specialist

Based in the Chicago area and reporting to the VP of Service and Applications, t...
Location
Location
United States , Chicago
Salary
Salary:
Not provided
focalone.com Logo
FOCAL ONE
Expiration Date
Until further notice
Flip Icon
Requirements
Requirements
  • 3+ years of ultrasound scanning experience in a patient care setting
  • Must pass an extensive background check and drug testing
  • Must have a clean driving record
  • Required immunizations/vaccinations: Hepatitis A & B, Chicken Pox, MMR Vaccine (Measles, Mumps & Rubella’s), Tetanus, Tuberculosis, and Influenza
  • Must have reliable transportation and possess a valid driver’s license
  • Must be physically fit and able to lift 30-50 pounds
  • Expert in product/clinical technical competencies, with the ability to answer a wide range of questions concerning software and clinical applications
Job Responsibility
Job Responsibility
  • Execution of customer training for the Company’s innovative technologies using ultrasound
  • Supports the US sales and service organizations along with EDAP’s market growth initiatives, including clinical presentations with potential new physician users
  • Provides a high level of customer satisfaction with training support and service, following manufacturer’s products requirements
  • Provides hands-on and didactic training at customer sites, to a physician and nursing audience, on products
  • Responsible for clinical training including didactic courses, case observations, product demonstrations and proctored case assistance
  • Provides consultative support to customers at every level, physician, nursing, sterile processing and OR managers
  • Coordinates the delivery of customer training with Service/Sales groups
  • Establishes and maintains a high level of customer satisfaction with manufacturer’s products thought continued training and case support
  • Maintains a good customer service reputation by complying with all regulatory requirements
  • Supports market growth initiatives (i.e. industry tradeshows, product demos, clinical sites)
What we offer
What we offer
  • Expense paid travel
  • EDAP will pay for required immunizations to be completed during first 60 days of employment if not up to date
  • Fulltime
Read More
Arrow Right
New

Senior Clinical Research Manager - Network Operations

The Senior Clinical Research Manager (CRM) provides strategic and operational ov...
Location
Location
United States , Brookline; Brighton; Milford; Weymouth; Methuen; Foxborough; Londonderry
Salary
Salary:
105400.00 - 130500.00 USD / Year
dana-farber.org Logo
Dana-Farber Cancer Institute
Expiration Date
Until further notice
Flip Icon
Requirements
Requirements
  • Bachelor’s Degree required, with a minimum of 7+ years of related experience or Master Degree with 5+ years experience.
  • Knowledge of cancer as a disease process, cancer treatment modalities, and the clinical trial process.
  • Experience in protocol development, data compilation and analysis.
  • Skilled at developing tracking systems to ensure timely data management by the clinical research staff.
  • Expert knowledge of Federal and State regulations as they relate to research.
  • Strong interpersonal, organizational and communication skills are required.
  • Must have computer skills including the use of Microsoft Office and working knowledge of Livelink
  • EPIC and OnCore applications.
  • Has expert knowledge of and is fully proficient in ability to execute clinical trials start-up, active and close out phases.
  • Is fully proficient in their knowledge of clinical research local policy and federal regulation.
Job Responsibility
Job Responsibility
  • CLINICAL TRIAL OPERATIONS: Responsible for the oversight of their disease group's clinical trial portfolio and all related regulatory, compliance and performance metrics requirements.
  • Oversee the processing of protocols through DFCI Institutional Review Board (and other institutions' IRBs) when appropriate.
  • Collaborate with the DFCI Clinical Trials Office (CTO), the Office for Human Research Studies (OHRS) and the Quality Assurance for Clinical Trials (QACT) to fulfill local and federal requirements governing human clinical trials.
  • Identify and manage operational, logistical, and regulatory challenges related to the conduct of clinical trials and acts as a leader in overseeing their resolution.
  • Assist the principal investigator in developing the protocol budget, in collaboration with Research Administration and the Grants and Contracts offices. Work with grant managers and other financial managers in the reporting and accounting of these funds.
  • Oversees and coordinates the purchase, receipt, inventory and distribution of equipment utilized in the conduct of clinical trials.
  • Work collaboratively with clinical research administration and grant managers to help monitor and reconcile all study and related grant finances as needed.
  • Assists the principal investigator in preparing manuscripts for publication.
  • Collaborate with the DFCI CTO and DF/HCC QACT to develop study forms, database information, and to establish guidelines for monitoring data quality control for PI Initiated studies / Multi-Center Trials
  • Oversee the subject enrollment, protocol treatment and follow-up care processes for protocol patients.
  • Fulltime
Read More
Arrow Right

Senior Clinical Application Specialist

Looking for an exciting challenge? A change in pace using your Rad Tech skill to...
Location
Location
Egypt , Cairo
Salary
Salary:
Not provided
paxerahealth.com Logo
PaxeraHealth
Expiration Date
Until further notice
Flip Icon
Requirements
Requirements
  • Excellent English Language
  • Experience as a radiology technologist or in similar clinical role
  • A deep understanding of medical imaging and the challenges faced by professionals in this industry
  • A Bachelor’s degree in Radiology, Biomedical Engineering or similar field
  • Strong presentation skills with sales ability
  • Ability to absorb and convey highly technical information
  • A hands-on and customer-centric approach
  • Must be able to travel to demonstrate to clients and to trade shows on occasion
  • Good time management skills and ability to prioritize tasks
  • Ability to work as part of a team
Job Responsibility
Job Responsibility
  • Serve as a software expert to clients and internal team members
  • Conduct webinars and workshops to demonstrate and provide technical expertise, support and training to clients as it relates to PaxeraHealth applications remotely and on-site
  • Create presentations, videos and other training materials as required for webinars, workshops and training sessions
  • Interfaces between clients/potential clients and company development team, skillfully forwarding pertinent suggestions and ideas to development for inclusion in future enhancements of software
  • Participate in the product development process
  • Develop and manage software documentation and technical support content including user manuals video-based tutorials and training tools
  • Attend conferences and exhibitions, meet with clients and demonstrate PaxeraHealth medical imaging solutions
  • Help with the product setup process as well as provide product presentations to customers and visitors during trade shows
  • Work together with technical teams and user groups to solve clients’ problems with available technology including hardware, software, databases and peripherals
  • Fulltime
Read More
Arrow Right

Clinical Services Manager

The Clinical Services Manager (Regulatory and Quality Compliance Lead) will play...
Location
Location
United Kingdom , Edgbaston or Glasgow
Salary
Salary:
55000.00 - 65000.00 GBP / Year
aces-eyeclinic.co.uk Logo
ACES Eye Clinic
Expiration Date
Until further notice
Flip Icon
Requirements
Requirements
  • Registered Healthcare Professional (NMC, HCPC, or equivalent)
  • Significant experience in clinical governance, regulatory compliance, or healthcare quality management
  • Strong understanding of CQC and UK regulatory frameworks, inspection preparation, and application processes
  • Skilled in data analysis, audit management, and quality reporting
  • Excellent communicator with the ability to engage confidently at senior and regulatory levels
  • Proactive, analytical, and organised, with a commitment to clinical excellence and patient safety
Job Responsibility
Job Responsibility
  • Lead on regulatory submissions, applications, and notifications to CQC and other UK regulators
  • Oversee governance administration, including Clinical Governance and Quality Committee meetings
  • Maintain and analyse the Quality and Compliance Dashboard to monitor clinical performance
  • Manage and report on incidents, complaints, investigations, and patient safety outcomes
  • Support and oversee compliance with mandatory training, clinical audits, and quality improvement plans
  • Undertake regular mock inspections and oversee our regulatory readiness framework
  • Liaise with commissioners, regulators, and internal stakeholders on matters of quality and compliance
  • Prepare comprehensive reports for the Director of Care and Quality and the Executive Team
  • Provide leadership and support to the Clinical Services Quality Team, promoting a culture of accountability and continuous improvement
What we offer
What we offer
  • 29 Days Annual leave
  • Private Medical Insurance
  • Free Eye surgery (LVC or IOL)
  • Discounts on other group procedures and goods
  • Fulltime
Read More
Arrow Right

Clinical Services Manager

The Clinical Services Manager (Regulatory and Quality Compliance Lead) will play...
Location
Location
United Kingdom , Glasgow; Edgbaston
Salary
Salary:
55000.00 - 65000.00 GBP / Year
aces-eyeclinic.co.uk Logo
ACES Eye Clinic
Expiration Date
Until further notice
Flip Icon
Requirements
Requirements
  • Registered Healthcare Professional (NMC, HCPC, or equivalent)
  • Significant experience in clinical governance, regulatory compliance, or healthcare quality management
  • Strong understanding of CQC and UK regulatory frameworks, inspection preparation, and application processes
  • Skilled in data analysis, audit management, and quality reporting
  • Excellent communicator with the ability to engage confidently at senior and regulatory levels
  • Proactive, analytical, and organised, with a commitment to clinical excellence and patient safety
Job Responsibility
Job Responsibility
  • Lead on regulatory submissions, applications, and notifications to CQC and other UK regulators
  • Oversee governance administration, including Clinical Governance and Quality Committee meetings
  • Maintain and analyse the Quality and Compliance Dashboard to monitor clinical performance
  • Manage and report on incidents, complaints, investigations, and patient safety outcomes
  • Support and oversee compliance with mandatory training, clinical audits, and quality improvement plans
  • Undertake regular mock inspections and oversee our regulatory readiness framework
  • Liaise with commissioners, regulators, and internal stakeholders on matters of quality and compliance
  • Prepare comprehensive reports for the Director of Care and Quality and the Executive Team
  • Provide leadership and support to the Clinical Services Quality Team, promoting a culture of accountability and continuous improvement
What we offer
What we offer
  • 29 Days Annual leave
  • Private Medical Insurance
  • Free Eye surgery (LVC or IOL)
  • Discounts on other group procedures and goods
  • Fulltime
Read More
Arrow Right

Manager, CSAR - Global Library

The Global Library Manager will report to the Sr. Manager, Clinical System and A...
Location
Location
India , Hyderabad
Salary
Salary:
Not provided
amgen.com Logo
Amgen
Expiration Date
Until further notice
Flip Icon
Requirements
Requirements
  • Master’s degree in life science, computer science, business administration or related field and 4 to 6 years of experience
  • Bachelor’s degree in life science, computer science, business administration or related field and 6 to 8 years of experience
  • Diploma in life science, computer science, business administration or related field and 10 to 12 years of experience
  • Broad knowledge / work experience in data management / programming in the Pharmaceutical or Biotech arena
  • General project management and planning experience
  • Experience in oversight of outside vendors (CRO’s, central labs, imaging vendors, IRT vendors, etc.)
  • Good Clinical Practice knowledge
  • Strong understanding and experience in the use of performance management techniques, measures, problem-solving and analytical thinking
  • Knowledge of drug development and clinical trials processes
  • Knowledge of data management processes
Job Responsibility
Job Responsibility
  • Support of clinical trial platform technologies
  • Support decision-making by acting as a data scientist bringing awareness to patterns and analytical insight
  • Leading and / or coordinating the definition of studies in clinical trial databases or clinical systems
  • Coordinating and providing programming support to Clinical Study Teams
  • Maintaining standard business processes within GDO to ensure compliance to regulatory bodies
  • Acting as a technical point of contact for systems deliverables on defined programs
  • Providing technical and business process input / expertise on new and emerging technologies
  • Develop, review and implement policies, SOPs and associated documents
  • Assist in preparing for and responding to audit findings (internal or external)
  • Provide Global Library review at the study level
What we offer
What we offer
  • Competitive and comprehensive Total Rewards Plans that are aligned with local industry standards
Read More
Arrow Right
Welcome to CrawlJobs.com
Your Global Job Discovery Platform
At CrawlJobs.com, we simplify finding your next career opportunity by bringing job listings directly to you from all corners of the web. Using cutting-edge AI and web-crawling technologies, we gather and curate job offers from various sources across the globe, ensuring you have access to the most up-to-date job listings in one place.